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Blue cone monochromacy is an inherited eye disease that causes severely impaired color discrimination, low vision, nystagmus and photophobia due to the absence of functionality of red and green cone photoreceptor cells in the retina. This form of retinal disorder is a recessive X-linked disease and manifests its symptoms in early infancy.
Blue cone monochromacy is considered a stationary disease, although there is evidence of disease progression with macular degeneration in many patients.
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